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HUM00087825 PROSPECTIVE, RANDOMIZED, DoubleClick, PLACEBOCONTROLLED TRIAL OF PROPHYLACTIC FOR POSTOPERATIVE URINARY RETENTION IN PRIMARY TOTAL HIP AND KNEE ARTHROPLASTY PATIENTSNCT02518971 IRB approved:
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Researchers and investigators conducting a study that falls under the scope of NCT02518971 IRB approved need to obtain this approval from the institutional review board. The approval ensures adherence to ethical standards and protection of human subjects participating in the study.
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What is nct02518971 irb approved?
NCT02518971 refers to a clinical trial registered on ClinicalTrials.gov, and 'IRB approved' indicates that it has been reviewed and approved by an Institutional Review Board to ensure that the study meets ethical standards.
Who is required to file nct02518971 irb approved?
The principal investigator or the lead research organization conducting the clinical trial is responsible for filing the IRB approval for NCT02518971.
How to fill out nct02518971 irb approved?
To fill out the IRB approval for NCT02518971, the principal investigator must complete the required forms detailing the study's purpose, methodology, participant safety measures, and obtain necessary signatures from the IRB.
What is the purpose of nct02518971 irb approved?
The purpose of obtaining IRB approval for NCT02518971 is to ensure the protection of the rights, welfare, and safety of human subjects participating in the clinical trial.
What information must be reported on nct02518971 irb approved?
The information that must be reported includes the study title, principal investigator details, study objectives, methodology, consent procedures, and any potential risks to participants.
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